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Results 1-10 of 39 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Familial partial epilepsy with variable foci: Clinical features and linkage to chromosome 22q12Berkovic, S.; Serratosa, J.; Phillips, H.; Xiong, L.; Andermann, E.; Diaz-Otero, F.; Gomez-Garre, P.; Martin, M.; Fernandez-Bullido, Y.; Andermann, F.; Lopes-Cendes, I.; Dubeau, F.; Desbiens, R.; Scheffer, I.; Wallace, R.; Mulley, J.; Pandolfo, M.
2003Channelopathies as a genetic cause of epilepsyMulley, J.; Scheffer, I.; Petrou, S.; Berkovic, S.
2007Reduced cortical inhibition in a mouse model of familial childhood absence epilepsyTan, H.; Reid, C.; Single, F.; Davies, P.; Chiu, C.; Murphy, S.; Clarke, A.; Dibbens, L.; Krestel, H.; Mulley, J.; Jones, M.; Seeburg, P.; Sakmann, B.; Berkovic, S.; Sprengel, R.; Petrou, S.
2002Sodium-channel defects in benign familial neonatal-infantile seizuresHeron, S.; Crossland, K.; Andermann, E.; Phillips, H.; Hall, A.; Bleasel, A.; Shevell, M.; Mercho, S.; Seni, M.; Guiot, M.; Mulley, J.; Berkovic, S.; Scheffer, I.
2007What is the role of genetics in epilepsy?Scheffer, I.; Dibbens, L.; Berkovic, S.; Mulley, J.; Sanjay Sisodiya,; Epilepsy Research Foundation workshop (6th : 2006 : Oxford, UK)
2000A de novo mutation in sporadic nocturnal frontal lobe epilepsyPhillips, H.; Marini, C.; Scheffer, I.; Sutherland, G.; Mulley, J.; Berkovic, S.
2005SCN1A mutations and epiliepsyMulley, J.; Scheffer, I.; Petrou, S.; Dibbens, L.; Berkovic, S.; Harkin, L.
2004Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathyBerkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2004Genetic association studies in epilepsy: The truth is out thereTan, N.; Mulley, J.; Berkovic, S.

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